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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381792Generated: November 2, 2026

Ethanol → Ethyl 3-methylthiophene-2-carboxylate

https://huagongshe.com/reaction/2381792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Methyl-2-thenoic acidHCID 90269—
ProductEthyl 3-methylthiophene-2-carboxylateHCID 1834793199%

Reaction Steps

To a stirred solution of 3-methylthiophene-2-carboxylic acid (5.00 g, 35.17 mmol) in ethanol (50 mL) was added thionyl chloride (2.60 mL, 35.62 mmol). The resulting reaction mixture was stirred at reflux for 16 h, and allowed to cool to ambient temperature and concentrated in vacuo. The residue was dissolved in ethyl acetate (200 mL) and washed with saturated aqueous sodium bicarbonate solution (3×100 mL) and brine (100 mL). The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to afford ethyl 3-methylthiophene-2-carboxylate as light yellow liquid (5.96 g, 99%): 1H NMR (300 MHz, CDCl3) δ 7.37 (d, J=5.0 Hz, 1H), 6.91 (d, J=5.0 Hz, 1H), 4.33 (q, J=7.1 Hz, 2H), 2.55 (s, 3H), 1.37 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258160B2
Source datasetuspto-grants-2012_09
ORD IDord-4cddbfcd0ef649778be051be287eb81a
Source noteuspto-grants-2012_09